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Tau Protein Assembles into Isoform- and Disulfide-dependent Polymorphic Fibrils with Distinct Structural Properties
Tauopathies are neurodegenerative diseases in which insoluble fibrillar aggregates of a microtubule-binding protein, Tau, are abnormally accumulated. Pathological Tau fibrils often exhibit structural polymorphisms that differ among phenotypically distinct tauopathies; however, a molecular mechanism...
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| Huvudupphovsmän: | , , |
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| Materialtyp: | Artigo |
| Språk: | Inglês |
| Publicerad: |
American Society for Biochemistry and Molecular Biology
2011
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| Länkar: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3149317/ https://ncbi.nlm.nih.gov/pubmed/21659525 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1074/jbc.M111.248963 |
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